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INNOSC Theranostics and
            Pharmacological Sciences                                                Anticancer activity of cyanobacteria



               agent and its preliminary evaluation in an orthotopic   expression and  suppresses  tumor  growth  in glioblastoma
               patient-derived xenograft (PDX) model. Invest New Drugs,   xenografts. Invest New Drugs, 34: 24–40.
               37: 364–374.
                                                                  https://doi.org/10.1007/s10637-015-0303-x
               https://doi.org/10.1007/s10637-018-0647-0
                                                               35.  Mooberry SL, Leal RM, Tinley TL, et al., 2003, The molecular
            25.  Gunasekera SP, Owle CS, Montaser R,  et al., 2011,   pharmacology of  symplostatin 1:  A  new antimitotic
               Malyngamide 3 and cocosamides A and B from the marine   dolastatin 10 analog. Int J Cancer, 104: 512–521.
               cyanobacterium  Lyngbya majuscula from Cocos Lagoon,      https://doi.org/10.1002/ijc.10982
               guam. J Nat Prod, 74: 871–876.
                                                               36.  MacMillan JB, Molinski TF, 2002, Caylobolide A, a unique
               https://doi.org/10.1021/np1008015
                                                                  36-membered macrolactone from a bahamian  Lyngbya
            26.  Michon S, Cavelier F, Salom-Roig XJ, 2021, Synthesis and   majuscula. Org Lett, 4: 1535–1538.
               biological activities of cyclodepsipeptides of aurilide family      https://doi.org/10.1021/ol025759p
               from marine origin. Mar Drugs, 19: 55.
                                                               37.  Salvador LA, Paul VJ, Luesch H, 2010, Caylobolide B, a
               https://doi.org/10.3390/md19020055
                                                                  macrolactone from  symplostatin  1-producing  marine
            27.  Han B, Gross H, Goeger DE, et al., 2006, Aurilides B and C,   Cyanobacteria Phormidium spp. from Florida. J Nat Prod,
               cancer cell toxins from a Papua new Guinea collection of   73: 1606–1609.
               the marine cyanobacterium Lyngbya majuscula. J Nat Prod,      https://doi.org/10.1021/np100467d
               69: 572–575.
                                                               38.  Tao Y, Li P, Zhang D, et al., 2018, Samholides, swinholide-
               https://doi.org/10.1021/np0503911
                                                                  related  metabolites from a  marine  Cyanobacterium  cf.
            28.  Robles-Bañuelos B, Durán-Riveroll LM, Rangel-López E,   Phormidium sp. J Org Chem, 83: 3034–3046.
               et al., 2022, Marine  Cyanobacteria as sources of lead      https://doi.org/10.1021/acs.joc.8b00028
               anticancer compounds: A review of families of metabolites
               with cytotoxic, antiproliferative, and antineoplastic effects.   39.  Afonso TB, Costa MS, Rezende De Castro R, et al., 2016,
               Molecules, 27: 4814.                               Bartolosides E-K from a marine coccoid cyanobacterium.
                                                                  J Nat Prod, 79: 2504–2513.
               https://doi.org/10.3390/molecules27154814
                                                                  https://doi.org/10.1021/acs.jnatprod.6b00351
            29.  Yao G, Wang W, Ao L, et al., 2018, Improved total synthesis
               and biological evaluation of coibamide A analogues. J Med   40.  Sasaki H, Teruya T, Fukazawa H, et al., 2011, Revised structure
               Chem, 61: 8808–8916.                               and structure-activity relationship of bisebromoamide
                                                                  and structure of norbisebromoamide from the marine
               https://doi.org/10.1021/acs.jmedchem.8b01141
                                                                  cyanobacterium Lyngbya sp. Tetrahedron, 67: 990–994.
            30.  Medina RA, Goeger DE, Hills P, et al., 2008, Coibamide A,   41.  Suzuki K, Mizuno R, Suenaga K, et al., 2013, Bisebromoamide,
               a potent antiproliferative cyclic depsipeptide from the   an extract from Lyngbya species, induces apoptosis through
               panamanian marine cyanobacterium Leptolyngbya sp. J Am   ERK and mTOR inhibitions in renal cancer cells.  Cancer
               Chem Soc, 130: 6324–6325.
                                                                  Med, 2: 32–39.
               https://doi.org/10.1021/ja801383f
                                                                  https://doi.org/10.1002/cam4.53
            31.  Kazemi S, Kawaguchi S, Badr CE,  et al., 2021, Targeting   42.  Johnston HJ, Boys SK, Makda A,  et al., 2016, Naturally
               of  HER/ErbB  family  proteins using broad  spectrum   inspired peptide leads: Alanine scanning reveals an
               Sec61 inhibitors coibamide A and apratoxin A.  Biochem   actin-targeting thiazole analogue of bisebromoamide.
               Pharmacol, 183: 114317.
                                                                  Chembiochem, 17: 1621–1627.
               https://doi.org/10.1016/j.bcp.2020.114317
                                                                  https://doi.org/10.1002/cbic.201600257
            32.  Shi W, Lu D, Wu C, et al., 2021, Coibamide A kills cancer   43.  Pereira AR, Kale AJ, Fenley AT,  et al., 2012, The
               cells through inhibiting autophagy.  Biochem Biophys Res   carmaphycins, new proteasome inhibitors exhibiting an
               Commun, 547: 52–58.
                                                                  α,β-epoxyketone warhead from a marine cyanobacterium.
               https://doi.org/10.1016/j.bbrc.2021.01.112         Chembiochem, 13: 810–817.
            33.  Tranter D, Paatero AO, Kawaguchi S, et al., 2020, Coibamide      https://doi.org/10.1002/cbic.201200007
               A targets Sec61 to prevent biogenesis of secretory and   44.  Brumley DA, Gunasekera SP, Chen QY,  et al., 2020,
               membrane proteins. ACS Chem Biol, 15: 2125–2136.
                                                                  Discovery, total synthesis and SAR of anaenamides A and B:
               https://doi.org/10.1021/acschembio.0c00325         Anticancer cyanobacterial depsipeptides with a chlorinated
                                                                  pharmacophore. Org Lett, 22: 4235–4239.
            34.  Serrill JD, Wan X, Hau AM,  et al., 2016, Coibamide A,
               a natural lariat depsipeptide, inhibits VEGFA/VEGFR2      https://doi.org/10.1021/acs.orglett.0c01281


            Volume 7 Issue 1 (2024)                         11                        https://doi.org/10.36922/itps.1388
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